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Volumn 388, Issue 2, 2009, Pages 260-265

Optimization of the enzymatic hydrolysis and analysis of plasma conjugated γ-CEHC and sulfated long-chain carboxychromanols, metabolites of vitamin E

Author keywords

CEHC; Glucuronidase; Metabolism; Sulfatase; Tocopherol; Tocotrienol

Indexed keywords

BIOMOLECULES; METABOLISM; METABOLITES; REACTION INTERMEDIATES; SULFUR COMPOUNDS;

EID: 64249159192     PISSN: 00032697     EISSN: 10960309     Source Type: Journal    
DOI: 10.1016/j.ab.2009.02.027     Document Type: Article
Times cited : (31)

References (27)
  • 1
    • 0036791124 scopus 로고    scopus 로고
    • Identities and differences in the metabolism of tocotrienols and tocopherols in HepG2 cells
    • Birringer M., Pfluger P., Kluth D., Landes N., and Brigelius-Flohe R. Identities and differences in the metabolism of tocotrienols and tocopherols in HepG2 cells. J. Nutr. 132 (2002) 3113-3118
    • (2002) J. Nutr. , vol.132 , pp. 3113-3118
    • Birringer, M.1    Pfluger, P.2    Kluth, D.3    Landes, N.4    Brigelius-Flohe, R.5
  • 2
    • 0033037413 scopus 로고    scopus 로고
    • Vitamin E: function and metabolism
    • Brigelius-Flohe R., and Traber M.G. Vitamin E: function and metabolism. FASEB J. 13 (1999) 1145-1155
    • (1999) FASEB J. , vol.13 , pp. 1145-1155
    • Brigelius-Flohe, R.1    Traber, M.G.2
  • 3
    • 0035185941 scopus 로고    scopus 로고
    • γ-Tocopherol, the major form of vitamin E in the US diet, deserves more attention
    • Jiang Q., Christen S., Shigenaga M.K., and Ames B.N. γ-Tocopherol, the major form of vitamin E in the US diet, deserves more attention. Am. J. Clin. Nutr. 74 (2001) 714-722
    • (2001) Am. J. Clin. Nutr. , vol.74 , pp. 714-722
    • Jiang, Q.1    Christen, S.2    Shigenaga, M.K.3    Ames, B.N.4
  • 4
    • 14944341755 scopus 로고    scopus 로고
    • Discovery, characterization, and significance of the cytochrome P450 omega-hydroxylase pathway of vitamin E catabolism
    • Parker R.S., Sontag T.J., Swanson J.E., and McCormick C.C. Discovery, characterization, and significance of the cytochrome P450 omega-hydroxylase pathway of vitamin E catabolism. Ann. NY Acad. Sci. 1031 (2004) 13-21
    • (2004) Ann. NY Acad. Sci. , vol.1031 , pp. 13-21
    • Parker, R.S.1    Sontag, T.J.2    Swanson, J.E.3    McCormick, C.C.4
  • 5
    • 0037067711 scopus 로고    scopus 로고
    • Cytochrome P450 omega-hydroxylase pathway of tocopherol catabolism: novel mechanism of regulation of vitamin E status
    • Sontag T.J., and Parker R.S. Cytochrome P450 omega-hydroxylase pathway of tocopherol catabolism: novel mechanism of regulation of vitamin E status. J. Biol. Chem. 277 (2002) 25290-25296
    • (2002) J. Biol. Chem. , vol.277 , pp. 25290-25296
    • Sontag, T.J.1    Parker, R.S.2
  • 6
    • 0021323645 scopus 로고
    • Novel urinary metabolite of d-δ-tocopherol in rats
    • Chiku S., Hamamura K., and Nakamura T. Novel urinary metabolite of d-δ-tocopherol in rats. J. Lipid Res. 25 (1984) 40-48
    • (1984) J. Lipid Res. , vol.25 , pp. 40-48
    • Chiku, S.1    Hamamura, K.2    Nakamura, T.3
  • 7
    • 0033662499 scopus 로고    scopus 로고
    • Production of LLU-α following an oral administration of γ-tocotrienol or γ-tocopherol to rats
    • Hattori A., Fukushima T., Yoshimura H., Abe K., and Imai K. Production of LLU-α following an oral administration of γ-tocotrienol or γ-tocopherol to rats. Biol. Pharm. Bull. 23 (2000) 1395-1397
    • (2000) Biol. Pharm. Bull. , vol.23 , pp. 1395-1397
    • Hattori, A.1    Fukushima, T.2    Yoshimura, H.3    Abe, K.4    Imai, K.5
  • 8
    • 0035113436 scopus 로고    scopus 로고
    • Α- and γ-tocotrienols are metabolized to carboxyethyl-hydroxychroman derivatives and excreted in human urine
    • Lodge J.K., Ridlington J., Leonard S., Vaule H., and Traber M.G. Α- and γ-tocotrienols are metabolized to carboxyethyl-hydroxychroman derivatives and excreted in human urine. Lipids 36 (2001) 43-48
    • (2001) Lipids , vol.36 , pp. 43-48
    • Lodge, J.K.1    Ridlington, J.2    Leonard, S.3    Vaule, H.4    Traber, M.G.5
  • 10
    • 0028858639 scopus 로고
    • Novel urinary metabolite of α-tocopherol, 2,5,7,8-tetramethyl-2(2′-carboxyethyl)-6-hydroxychroman, as an indicator of an adequate vitamin E supply?
    • Schultz M., Leist M., Petrzika M., Gassmann B., and Brigelius-Flohe R. Novel urinary metabolite of α-tocopherol, 2,5,7,8-tetramethyl-2(2′-carboxyethyl)-6-hydroxychroman, as an indicator of an adequate vitamin E supply?. Am. J. Clin. Nutr. 62 (1995) 1527S-1534S
    • (1995) Am. J. Clin. Nutr. , vol.62
    • Schultz, M.1    Leist, M.2    Petrzika, M.3    Gassmann, B.4    Brigelius-Flohe, R.5
  • 11
    • 0032933234 scopus 로고    scopus 로고
    • Urinary excretion of 2,7,8-trimethyl-2-(β-carboxyethyl)-6-hydroxychroman is a major route of elimination of γ-tocopherol in humans
    • Swanson J.E., Ben R.N., Burton G.W., and Parker R.S. Urinary excretion of 2,7,8-trimethyl-2-(β-carboxyethyl)-6-hydroxychroman is a major route of elimination of γ-tocopherol in humans. J. Lipid Res. 40 (1999) 665-671
    • (1999) J. Lipid Res. , vol.40 , pp. 665-671
    • Swanson, J.E.1    Ben, R.N.2    Burton, G.W.3    Parker, R.S.4
  • 12
    • 0032538402 scopus 로고    scopus 로고
    • Synthetic as compared with natural vitamin E is preferentially excreted as α-CEHC in human urine: studies using deuterated α-tocopheryl acetates
    • Traber M.G., Elsner A., and Brigelius-Flohe R. Synthetic as compared with natural vitamin E is preferentially excreted as α-CEHC in human urine: studies using deuterated α-tocopheryl acetates. FEBS Lett. 437 (1998) 145-148
    • (1998) FEBS Lett. , vol.437 , pp. 145-148
    • Traber, M.G.1    Elsner, A.2    Brigelius-Flohe, R.3
  • 14
    • 67649690494 scopus 로고    scopus 로고
    • J.Y. Cho, D. Wook Kang, X. Ma, S.H. Ahn, K.W. Krausz, H. Luecke, J.R. Idle, F.J. Gonzalez, Metabolomics reveals a novel vitamin E metabolite and attenuated vitamin E metabolism upon PXR activation, J. Lipid Res. 2009 [Epub ahead of print].
    • J.Y. Cho, D. Wook Kang, X. Ma, S.H. Ahn, K.W. Krausz, H. Luecke, J.R. Idle, F.J. Gonzalez, Metabolomics reveals a novel vitamin E metabolite and attenuated vitamin E metabolism upon PXR activation, J. Lipid Res. 2009 [Epub ahead of print].
  • 15
    • 65349107677 scopus 로고    scopus 로고
    • γ-Tocotrienol and γ-tocopherol are primarily metabolized to conjugated 2-(β-carboxyethyl)-6-hydroxychroman and sulfated long-chain carboxychromanols in rats
    • in press
    • H. Freiser, Q. Jiang, γ-Tocotrienol and γ-tocopherol are primarily metabolized to conjugated 2-(β-carboxyethyl)-6-hydroxychroman and sulfated long-chain carboxychromanols in rats, J. Nutr. (2009), in press.
    • (2009) J. Nutr
    • Freiser, H.1    Jiang, Q.2
  • 16
    • 34248183943 scopus 로고    scopus 로고
    • Identification and quantitation of novel vitamin E metabolites, sulfated long-chain carboxychromanols, in human A549 cells and in rats
    • Jiang Q., Freiser H., Wood K.V., and Yin X. Identification and quantitation of novel vitamin E metabolites, sulfated long-chain carboxychromanols, in human A549 cells and in rats. J. Lipid Res. 48 (2007) 1221-1230
    • (2007) J. Lipid Res. , vol.48 , pp. 1221-1230
    • Jiang, Q.1    Freiser, H.2    Wood, K.V.3    Yin, X.4
  • 17
    • 58149488676 scopus 로고    scopus 로고
    • Long-chain carboxychromanols, metabolites of vitamin E, are potent inhibitors of cyclooxygenases
    • Jiang Q., Yin X., Lill M.A., Danielson M.L., Freiser H., and Huang J. Long-chain carboxychromanols, metabolites of vitamin E, are potent inhibitors of cyclooxygenases. Proc. Natl. Acad. Sci. USA 105 (2008) 20464-20469
    • (2008) Proc. Natl. Acad. Sci. USA , vol.105 , pp. 20464-20469
    • Jiang, Q.1    Yin, X.2    Lill, M.A.3    Danielson, M.L.4    Freiser, H.5    Huang, J.6
  • 18
    • 27244433672 scopus 로고    scopus 로고
    • Quantitation of rat liver vitamin E metabolites by LC-MS during high-dose vitamin E administration
    • Leonard S.W., Gumpricht E., Devereaux M.W., Sokol R.J., and Traber M.G. Quantitation of rat liver vitamin E metabolites by LC-MS during high-dose vitamin E administration. J. Lipid Res. 46 (2005) 1068-1075
    • (2005) J. Lipid Res. , vol.46 , pp. 1068-1075
    • Leonard, S.W.1    Gumpricht, E.2    Devereaux, M.W.3    Sokol, R.J.4    Traber, M.G.5
  • 19
    • 0033983850 scopus 로고    scopus 로고
    • A rapid method for the extraction and determination of vitamin E metabolites in human urine
    • Lodge J.K., Traber M.G., Elsner A., and Brigelius-Flohe R. A rapid method for the extraction and determination of vitamin E metabolites in human urine. J. Lipid Res. 41 (2000) 148-154
    • (2000) J. Lipid Res. , vol.41 , pp. 148-154
    • Lodge, J.K.1    Traber, M.G.2    Elsner, A.3    Brigelius-Flohe, R.4
  • 20
    • 0033571604 scopus 로고    scopus 로고
    • Quantification of the α- and γ-tocopherol metabolites 2,5,7,8-tetramethyl-2-(2′-carboxyethyl)-6-hydroxychroman and 2,7,8-trimethyl-2-(2′-carboxyethyl)-6-hydroxychroman in human serum
    • Stahl W., Graf P., Brigelius-Flohe R., Wechter W., and Sies H. Quantification of the α- and γ-tocopherol metabolites 2,5,7,8-tetramethyl-2-(2′-carboxyethyl)-6-hydroxychroman and 2,7,8-trimethyl-2-(2′-carboxyethyl)-6-hydroxychroman in human serum. Anal. Biochem. 275 (1999) 254-259
    • (1999) Anal. Biochem. , vol.275 , pp. 254-259
    • Stahl, W.1    Graf, P.2    Brigelius-Flohe, R.3    Wechter, W.4    Sies, H.5
  • 21
    • 19444373834 scopus 로고    scopus 로고
    • Optimization of conditions for the enzymatic hydrolysis of phytoestrogen conjugates in urine and plasma
    • Taylor J.I., Grace P.B., and Bingham S.A. Optimization of conditions for the enzymatic hydrolysis of phytoestrogen conjugates in urine and plasma. Anal. Biochem. 341 (2005) 220-229
    • (2005) Anal. Biochem. , vol.341 , pp. 220-229
    • Taylor, J.I.1    Grace, P.B.2    Bingham, S.A.3
  • 23
    • 0036721557 scopus 로고    scopus 로고
    • Pharmacokinetics of the glucuronide and sulfate conjugates of genistein and daidzein in men and women after consumption of a soy beverage
    • Shelnutt S.R., Cimino C.O., Wiggins P.A., Ronis M.J., and Badger T.M. Pharmacokinetics of the glucuronide and sulfate conjugates of genistein and daidzein in men and women after consumption of a soy beverage. Am. J. Clin. Nutr. 76 (2002) 588-594
    • (2002) Am. J. Clin. Nutr. , vol.76 , pp. 588-594
    • Shelnutt, S.R.1    Cimino, C.O.2    Wiggins, P.A.3    Ronis, M.J.4    Badger, T.M.5
  • 24
    • 0035053321 scopus 로고    scopus 로고
    • Comparison of the rates of hydrolysis of lorazepam-glucuronide, oxazepam-glucuronide, and tamazepam-glucuronide catalyzed by E. coli β-d-glucuronidase using the on-line benzodiazepine screening immunoassay on the Roche/Hitachi 917 analyzer
    • Dou C., Bournique J.S., Zinda M.K., Gnezda M., McNally A.J., and Salamone S.J. Comparison of the rates of hydrolysis of lorazepam-glucuronide, oxazepam-glucuronide, and tamazepam-glucuronide catalyzed by E. coli β-d-glucuronidase using the on-line benzodiazepine screening immunoassay on the Roche/Hitachi 917 analyzer. J. Forensic Sci. 46 (2001) 335-340
    • (2001) J. Forensic Sci. , vol.46 , pp. 335-340
    • Dou, C.1    Bournique, J.S.2    Zinda, M.K.3    Gnezda, M.4    McNally, A.J.5    Salamone, S.J.6
  • 25
    • 0034836384 scopus 로고    scopus 로고
    • Hydrolysis of conjugated steroids by the combined use of β-glucuronidase preparations from Helix pomatia and ampullaria: determination of urinary cortisol and its metabolites
    • Shibasaki H., Tanabe C., Furuta T., and Kasuya Y. Hydrolysis of conjugated steroids by the combined use of β-glucuronidase preparations from Helix pomatia and ampullaria: determination of urinary cortisol and its metabolites. Steroids 66 (2001) 795-801
    • (2001) Steroids , vol.66 , pp. 795-801
    • Shibasaki, H.1    Tanabe, C.2    Furuta, T.3    Kasuya, Y.4
  • 26
    • 0034972661 scopus 로고    scopus 로고
    • Α-Tocopherol affects the urinary and biliary excretion of 2,7,8-trimethyl-2(2′-carboxyethyl)-6-hydroxychroman, γ-tocopherol metabolite, in rats
    • Kiyose C., Saito H., Kaneko K., Hamamura K., Tomioka M., Ueda T., and Igarashi O. Α-Tocopherol affects the urinary and biliary excretion of 2,7,8-trimethyl-2(2′-carboxyethyl)-6-hydroxychroman, γ-tocopherol metabolite, in rats. Lipids 36 (2001) 467-472
    • (2001) Lipids , vol.36 , pp. 467-472
    • Kiyose, C.1    Saito, H.2    Kaneko, K.3    Hamamura, K.4    Tomioka, M.5    Ueda, T.6    Igarashi, O.7
  • 27
    • 9944239748 scopus 로고    scopus 로고
    • Intravenous administration of 2,7,8-trimethyl-2-(β-carboxyethyl)-6-hydroxy chroman (γ-CEHC) to rats and determination of its plasma concentration and urinary sodium excretion
    • Tanabe M., Fukushima T., Usui N., Aoyama N., Tsunoda M., and Imai K. Intravenous administration of 2,7,8-trimethyl-2-(β-carboxyethyl)-6-hydroxy chroman (γ-CEHC) to rats and determination of its plasma concentration and urinary sodium excretion. Biomed. Chromatogr. 18 (2004) 727-734
    • (2004) Biomed. Chromatogr. , vol.18 , pp. 727-734
    • Tanabe, M.1    Fukushima, T.2    Usui, N.3    Aoyama, N.4    Tsunoda, M.5    Imai, K.6


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